Actively Recruiting
Research and Clinical Validation of a Wearable Device-Based Remote Rehabilitation System for Postoperative Rotator Cuff Injury
Led by Peking University Third Hospital · Updated on 2026-03-10
72
Participants Needed
1
Research Sites
101 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study included patients who underwent their first shoulder rotator cuff surgery at Peking University Third Hospital, diagnosed with small to medium rotator cuff tears based on MRI results. Participants were randomly divided into an online wearable device training group and an offline traditional rehabilitation group, with 36 individuals in each group. Before testing began, patients were ensured to participate voluntarily and had signed informed consent forms.
CONDITIONS
Official Title
Research and Clinical Validation of a Wearable Device-Based Remote Rehabilitation System for Postoperative Rotator Cuff Injury
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- First-time rotator cuff surgery performed at Peking University Third Hospital
- MRI confirmed rotator cuff tear with a maximum diameter less than 3 cm by at least three musculoskeletal rehabilitation radiologists
- Own a mobile device with internet access capable of using mobile applications
- Able to complete the study and follow-ups within 6 months after discharge
- No visual, hearing, cognitive, or communication impairments
- Able to provide informed and valid consent to participate in the study
You will not qualify if you...
- Presence of serious cardiovascular or cerebrovascular diseases or cervical spondylosis with nerve damage
- Cognitive impairment or vision problems
- Stroke, rheumatic disease, neurological disorders, or diseases limiting overall physical or cardiopulmonary function within the past 2 years
- No prior history of shoulder joint injury and having undergone other surgeries within the past 6 months
- Unable to complete the entire study cycle or dropout during the study
- Serious postoperative complications such as wound infection or venous thromboembolism
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Peking University Third Hospital
Beijing, China
Actively Recruiting
Research Team
S
Shuang Ren, Doctor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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